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rs11568563

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11568563(A;C)
Make rs11568563(C;C)
ReferenceGRCh38 38.1/142
Chromosome12
Position21304500
GeneSLCO1A2
is asnp
is mentioned by
dbSNPrs11568563
ebirs11568563
HLIrs11568563
Exacrs11568563
Varsomers11568563
Maprs11568563
PheGenIrs11568563
hapmaprs11568563
1000 genomesrs11568563
hgdprs11568563
ensemblrs11568563
gopubmedrs11568563
geneviewrs11568563
scholarrs11568563
googlers11568563
pharmgkbrs11568563
gwascentralrs11568563
openSNPrs11568563
23andMers11568563
23andMe allrs11568563
SNP Nexus

SNPshotrs11568563
SNPdbers11568563
MSV3drs11568563
GWAS Ctlgrs11568563
GMAF0.03352
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21685912OA-icon.png]
Trait
Title Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Risk Allele
P-val 7E-8
Odds Ratio 1.4700 [1.28-1.69]


GET Evidence
SLCO1A2-E172D
aa_change Glu172Asp
aa_change_short E172D
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.04248
summary